NM_000106.6:c.1012G>A

HGVS Expressions

  • NG_008376.3:g.7384G>A
  • NM_000106.6:c.1012G>A
  • NP_000097.3:p.Val338Met
  • NC_000022.11:g.42127608C>T
Back to search Result
Clinvar Clinical Significance

Likely Benign

CTGA Clinical Significance

Drug Response

Variant Type

Substitution

Clinvar

598263

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
608902.G.1.4United Arab EmiratesDrug ResponseDrug Metabolism, Poor, CYP2D6-RelatedQumsieh et al. 2011 Subset of 608902.G.1.1. Number of subjec...
© CAGS 2024. All rights reserved.